Manufacturing Technician III

Job Title:

Manufacturing Technician III Job Description The Manufacturing Technician III (Compound/Fill/Finish) plays a crucial role in a fast-paced environment, assisting with the manufacturing of sterile injectable products in vial and syringe configurations for clinical and commercial distribution. This position involves overseeing and executing advanced production tasks using aseptic isolator technology. The role requires a high level of technical expertise in aseptic processes, strong leadership in troubleshooting, and a commitment to maintaining quality and compliance with Good Manufacturing Practices (GMP). The technician will operate manufacturing processing equipment following standard operating procedures and batch records, ensuring compliance with regulatory agencies and current Good Manufacturing Practices (cGMPs). Responsibilities Perform complex manufacturing operations, including setup, operation, and maintenance of equipment used in dispensing, compounding, filling (isolators), and visual inspection. Serve as a subject matter expert on compounding/filling processes and equipment, providing guidance and training to other manufacturing employees. Monitor production processes to ensure adherence to SOPs, batch records, and quality standards, making real-time adjustments to maintain product quality. Troubleshoot and resolve complex equipment and process issues, minimizing downtime and ensuring efficient production flow. Conduct in-process and end-of-process sampling/quality checks, ensuring all manufactured products meet rigorous standards. Collaborate with cross-functional teams on continuous improvement initiatives to enhance product quality, safety, and efficiency. Act as an active team member, enacting ideas and incorporating them as part of manufacturing readiness and execution. Assist with the validation and qualification of new equipment and processes, ensuring seamless integration into the production workflow. Maintain accurate and detailed production documentation, completing it with minimum errors and recommending revisions to reduce errors. Follow applicable SOPs and cGMPs to perform assigned duties and tasks. Ensure timely completion and compliance with cGMP and all other relevant company training requirements. Legibly document activities in real time on controlled documentation per SOPs and cGMPs. Perform in-process sampling, weight checks, and component counting and basic math calculations. Perform in-process inspection and finished product visual inspection. Clean rooms, tools, and equipment before and after use. Assist with other manufacturing areas as required. Perform activities right the first time in areas of material handling/dispensing, compounding, and filling. Follow general instructions on routine work and detailed instructions on new projects or assignments. Follow all safety requirements and lead by example a safety-first culture. Work occasional hours outside of scheduled shift based on business needs, which may include weekend work. Essential Skills 4-6+ years of relevant experience in sterile/aseptic manufacturing or Drug Substance manufacturing. Experience in a cGMP pharmaceutical manufacturing environment. Proven ability to operate, troubleshoot, and maintain complex manufacturing equipment. Demonstrated leadership skills with experience training and mentoring team members. Strong analytical and problem-solving skills with a focus on detail and accuracy. Excellent verbal and written communication skills, capable of working collaboratively in a team environment. Ability to read and comprehend detailed written instructions and apply instructions during execution. Basic computer skills (Microsoft Office) and familiarity with electronic documentation systems. Additional Skills & Qualifications High school diploma or GED required. Associate's or Bachelor's degree preferred. Prior pharmaceutical or CDMO experience. Work Environment This is a 100% on-site position, requiring work during the 3rd shift from Sunday to Thursday, 11:00 pm to 7:30 am. Employees must use appropriate personal protective equipment (PPE) based on the product, such as PAPR or Supplied Air Respirator. The role involves working in a manufacturing environment where adherence to safety and aseptic techniques is critical. Occasional work outside of scheduled shifts, including weekends, may be required based on business needs. Job Type & Location This is a Permanent position based out of Morrisville, NC. Pay and Benefits The pay range for this position is $62400.00 - $79040.00/yr. Competitive salary, and an exceptional benefits package including medical, dental, vision and prescription coverage, life, LTD, STD, 401(k) with match and immediate vesting, and tuition reimbursement / student loan forgiveness. Workplace Type This is a fully onsite position in Morrisville,NC. Application Deadline This position is anticipated to close on Mar 31, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our people Actalent is an equal opportunity employer. About Actalent Actalent is a global leader in engineering and sciences services. For more than 40 years, we've helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.